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Diagnostic potential of TERT promoter and FGFR3 mutations in urinary cell‐free DNA in upper tract urothelial carcinoma

机译:TERT启动子和FGFR3基因突变在上尿路上皮癌中的诊断潜力

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摘要

Most upper tract urothelial carcinomas (UTUC) are muscle invasive at the time of diagnosis. Current standard methods for the diagnosis of UTUC are invasive. Urine cytology is the only non‐invasive test for detecting UTUC, but its sensitivity is low. A novel non‐invasive assay for UTUC detection would improve patient outcome. This study aimed to investigate the mutation of cell‐free DNA (cfDNA) in urine supernatant to develop a reliable diagnostic biomarker for UTUC patients. We studied urinary cfDNA from 153 individuals, including 56 patients with localized UTUC, and carried out droplet digital PCR assay for TERT promoter and FGFR3 hotspot mutations. We could detect mutations of TERT C228T in 22/56 (39.3%), TERT C250T in 4/56 (7.1%), and FGFR3 S249C in 9/56 (16.1%) patients. FGFR3 mutation was detected only in ≤ style="fixed-case">pT1 tumors (positive predictive value: 100.0%). In combination with cytology results, the sensitivity was 78.6%, and the specificity was 96.0%. Although these data need to be validated in a larger‐scale cohort, mutation analysis of style="fixed-case">TERT promoter and style="fixed-case">FGFR3 in urinary cf style="fixed-case">DNA has the potential to be a non‐invasive diagnostic marker and reliable factor for tumor staging.
机译:在诊断时,大多数上尿路尿路上皮癌(UTUC)是浸润性的。当前用于诊断UTUC的标准方法是侵入性的。尿液细胞学检查是唯一可检测UTUC的非侵入性检查,但其敏感性较低。一种用于UTUC检测的新型无创检测方法将改善患者预后。这项研究旨在研究尿液上清液中无细胞DNA(cfDNA)的突变,从而为UTUC患者开发可靠的诊断生物标志物。我们研究了153例患者的尿cfDNA,包括56例局部UTUC患者,并对TERT启动子和FGFR3热点突变进行了液滴数字PCR分析。我们可以检测到22/56(39.3%)的TERT C228T突变,4/56(7.1%)的TERT C250T和9/56(16.1%)的FGFR3 S249C突变。仅在≤ style =“ fixed-case”> pT 1肿瘤中检测到FGFR3突变(阳性预测值:100.0%)。结合细胞学结果,敏感性为78.6%,特异性为96.0%。尽管这些数据需要在更大范围的队列中进行验证,但是对 style =“ fixed-case”> TERT 启动子和 style =“ fixed-case”> FGFR 3的突变分析尿中的cf style =“ fixed-case”> DNA 具有成为非侵入性诊断标志物和肿瘤分期可靠因素的潜力。

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